Evidence map›Paper›PMID 41425860›Full record

ArticleMethodsX2025

TARGETFLOW:An automated literature mining pipeline for accelerating the discovery of high-potential targets in rare and mature diseases.

Shuhan Guo, Tianxiang Shang, Yuzhu Pan, Yingjia Wu, Yan Li, Mohan Zhou

Abstract read
In one paragraph

Article in MethodsX, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Shuhan GuoSchool of Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu 211198, China.
Tianxiang ShangSchool of Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu 211198, China.
Yuzhu PanSchool of Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu 211198, China.
Yingjia WuSchool of Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu 211198, China.
Yan LiSchool of Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu 211198, China.
Mohan ZhouSchool of Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu 211198, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To expedite the early stages of drug development for diseases lacking established target databases, and to enhance knowledge updating in well-studied disease domains, this paper introduces TARGETFLOW, an automated literature-mining pipeline. The workflow begins by automatically retrieving literature, downloading relevant abstracts, and constructing a comprehensive database. After performing selective text cleaning and data preprocessing, it leverages large language models (LLMs) to conduct intelligent literature screening, followed by code-based whitespace tokenization. Subsequently, rule-based filtering is applied to extract high-potential therapeutic targets for the specified disease. To validate the effectiveness of this pipeline, three hypotheses were formulated: (1) An effective pipeline should be capable of identifying high-potential therapeutic targets for the given disease; (2) For diseases with established target databases, the pipeline should be able to detect novel and emerging targets not yet included in existing databases; and (3) The pipeline should also be applicable to rare or emerging diseases that lack mature target databases. Then, rheumatoid arthritis (RA), a common disease, and idiopathic pulmonary fibrosis (IPF), a rare disease, were selected as case studies. The results demonstrated the method's reliability (high-potential target validation rate: 56 %), innovativeness (new target validation pass rate: 100 %), and generalizability (IPF target literature support rate: 88.9 %).

Indexed as

Automated pipelineLiterature miningNamed entity recognitionNatural language processingRare diseasesTargets discovery

Identifiers

PMID41425860
PMCPMC12712683

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.